GB2483555A - Diaphragm Electrolyser for Disinfectant Production - Google Patents
Diaphragm Electrolyser for Disinfectant Production Download PDFInfo
- Publication number
- GB2483555A GB2483555A GB1115467.1A GB201115467A GB2483555A GB 2483555 A GB2483555 A GB 2483555A GB 201115467 A GB201115467 A GB 201115467A GB 2483555 A GB2483555 A GB 2483555A
- Authority
- GB
- United Kingdom
- Prior art keywords
- cathode
- anode
- electrolyser
- chamber
- flow
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Withdrawn
Links
- 239000000645 desinfectant Substances 0.000 title claims abstract description 53
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 7
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 claims abstract description 66
- 239000011780 sodium chloride Substances 0.000 claims abstract description 33
- 239000013505 freshwater Substances 0.000 claims abstract description 26
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 19
- 239000001257 hydrogen Substances 0.000 claims abstract description 6
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 6
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 5
- 238000000034 method Methods 0.000 claims description 59
- 239000003792 electrolyte Substances 0.000 claims description 50
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 40
- 239000000460 chlorine Substances 0.000 claims description 40
- 229910052801 chlorine Inorganic materials 0.000 claims description 40
- 150000001805 chlorine compounds Chemical class 0.000 claims description 7
- 239000007864 aqueous solution Substances 0.000 claims description 6
- 238000005868 electrolysis reaction Methods 0.000 claims description 6
- 230000008878 coupling Effects 0.000 claims description 4
- 238000010168 coupling process Methods 0.000 claims description 4
- 238000005859 coupling reaction Methods 0.000 claims description 4
- 238000007599 discharging Methods 0.000 claims description 4
- 150000002431 hydrogen Chemical class 0.000 claims 1
- 230000000249 desinfective effect Effects 0.000 abstract description 9
- 239000007788 liquid Substances 0.000 abstract description 3
- 239000000498 cooling water Substances 0.000 abstract 1
- 239000000243 solution Substances 0.000 description 16
- 238000001816 cooling Methods 0.000 description 13
- 230000008569 process Effects 0.000 description 7
- 230000009467 reduction Effects 0.000 description 7
- 150000003839 salts Chemical class 0.000 description 7
- 239000000126 substance Substances 0.000 description 6
- 239000012530 fluid Substances 0.000 description 5
- 239000000463 material Substances 0.000 description 5
- 238000010276 construction Methods 0.000 description 4
- 238000005520 cutting process Methods 0.000 description 3
- 238000005516 engineering process Methods 0.000 description 3
- 238000012423 maintenance Methods 0.000 description 3
- 230000007935 neutral effect Effects 0.000 description 3
- 238000004458 analytical method Methods 0.000 description 2
- 230000033558 biomineral tissue development Effects 0.000 description 2
- 230000003247 decreasing effect Effects 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000010292 electrical insulation Methods 0.000 description 2
- 230000007717 exclusion Effects 0.000 description 2
- ZZUFCTLCJUWOSV-UHFFFAOYSA-N furosemide Chemical compound C1=C(Cl)C(S(=O)(=O)N)=CC(C(O)=O)=C1NCC1=CC=CO1 ZZUFCTLCJUWOSV-UHFFFAOYSA-N 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 230000001105 regulatory effect Effects 0.000 description 2
- 239000013049 sediment Substances 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- FKNQFGJONOIPTF-UHFFFAOYSA-N Sodium cation Chemical compound [Na+] FKNQFGJONOIPTF-UHFFFAOYSA-N 0.000 description 1
- 238000009825 accumulation Methods 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 238000007743 anodising Methods 0.000 description 1
- 230000033228 biological regulation Effects 0.000 description 1
- 238000004364 calculation method Methods 0.000 description 1
- 238000003889 chemical engineering Methods 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 230000003292 diminished effect Effects 0.000 description 1
- 238000003487 electrochemical reaction Methods 0.000 description 1
- 230000002708 enhancing effect Effects 0.000 description 1
- 230000036541 health Effects 0.000 description 1
- QWPPOHNGKGFGJK-UHFFFAOYSA-N hypochlorous acid Chemical compound ClO QWPPOHNGKGFGJK-UHFFFAOYSA-N 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 235000013372 meat Nutrition 0.000 description 1
- 230000005012 migration Effects 0.000 description 1
- 238000013508 migration Methods 0.000 description 1
- 239000008267 milk Substances 0.000 description 1
- 210000004080 milk Anatomy 0.000 description 1
- 235000013336 milk Nutrition 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 239000007800 oxidant agent Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 230000003449 preventive effect Effects 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- UKLNMMHNWFDKNT-UHFFFAOYSA-M sodium chlorite Chemical compound [Na+].[O-]Cl=O UKLNMMHNWFDKNT-UHFFFAOYSA-M 0.000 description 1
- 229960002218 sodium chlorite Drugs 0.000 description 1
- 229910001415 sodium ion Inorganic materials 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 230000009182 swimming Effects 0.000 description 1
- 239000002351 wastewater Substances 0.000 description 1
- 238000004065 wastewater treatment Methods 0.000 description 1
- 239000012224 working solution Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
- C25B—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES FOR THE PRODUCTION OF COMPOUNDS OR NON-METALS; APPARATUS THEREFOR
- C25B1/00—Electrolytic production of inorganic compounds or non-metals
- C25B1/01—Products
- C25B1/24—Halogens or compounds thereof
- C25B1/26—Chlorine; Compounds thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L2/00—Methods or apparatus for disinfecting or sterilising materials or objects other than foodstuffs or contact lenses; Accessories therefor
- A61L2/16—Methods or apparatus for disinfecting or sterilising materials or objects other than foodstuffs or contact lenses; Accessories therefor using chemical substances
- A61L2/18—Liquid substances or solutions comprising solids or dissolved gases
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F1/00—Treatment of water, waste water, or sewage
- C02F1/46—Treatment of water, waste water, or sewage by electrochemical methods
- C02F1/461—Treatment of water, waste water, or sewage by electrochemical methods by electrolysis
- C02F1/46104—Devices therefor; Their operating or servicing
- C02F1/46109—Electrodes
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F1/00—Treatment of water, waste water, or sewage
- C02F1/46—Treatment of water, waste water, or sewage by electrochemical methods
- C02F1/461—Treatment of water, waste water, or sewage by electrochemical methods by electrolysis
- C02F1/467—Treatment of water, waste water, or sewage by electrochemical methods by electrolysis by electrochemical disinfection; by electrooxydation or by electroreduction
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F1/00—Treatment of water, waste water, or sewage
- C02F1/46—Treatment of water, waste water, or sewage by electrochemical methods
- C02F1/461—Treatment of water, waste water, or sewage by electrochemical methods by electrolysis
- C02F1/467—Treatment of water, waste water, or sewage by electrochemical methods by electrolysis by electrochemical disinfection; by electrooxydation or by electroreduction
- C02F1/4672—Treatment of water, waste water, or sewage by electrochemical methods by electrolysis by electrochemical disinfection; by electrooxydation or by electroreduction by electrooxydation
- C02F1/4674—Treatment of water, waste water, or sewage by electrochemical methods by electrolysis by electrochemical disinfection; by electrooxydation or by electroreduction by electrooxydation with halogen or compound of halogens, e.g. chlorine, bromine
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F2201/00—Apparatus for treatment of water, waste water or sewage
- C02F2201/002—Construction details of the apparatus
- C02F2201/003—Coaxial constructions, e.g. a cartridge located coaxially within another
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F2201/00—Apparatus for treatment of water, waste water or sewage
- C02F2201/46—Apparatus for electrochemical processes
- C02F2201/461—Electrolysis apparatus
- C02F2201/46105—Details relating to the electrolytic devices
- C02F2201/4612—Controlling or monitoring
- C02F2201/46145—Fluid flow
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F2201/00—Apparatus for treatment of water, waste water or sewage
- C02F2201/46—Apparatus for electrochemical processes
- C02F2201/461—Electrolysis apparatus
- C02F2201/46105—Details relating to the electrolytic devices
- C02F2201/46155—Heating or cooling
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F2209/00—Controlling or monitoring parameters in water treatment
- C02F2209/06—Controlling or monitoring parameters in water treatment pH
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Electrochemistry (AREA)
- Engineering & Computer Science (AREA)
- Organic Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Hydrology & Water Resources (AREA)
- Environmental & Geological Engineering (AREA)
- Water Supply & Treatment (AREA)
- Health & Medical Sciences (AREA)
- Inorganic Chemistry (AREA)
- Materials Engineering (AREA)
- Metallurgy (AREA)
- Epidemiology (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Water Treatment By Electricity Or Magnetism (AREA)
- Electrolytic Production Of Non-Metals, Compounds, Apparatuses Therefor (AREA)
Abstract
An electrolyser for disinfectant production comprises a hollow cylindrical cathode 20 through which fresh water is channelled. A cathode chamber is defined between the outer surface of the cathode and an inner surface of a coaxial diaphragm 80 and an anode chamber 32 is defined between the outer surface of the diaphragm and a cylindrical anode 50 coaxially surrounding it. A cover mixer 30 at the upper end of the cell has an internal annular mixing channel 33 in communication with the upper end of the anode chamber, with a water inlet 31 and an outlet 34 from which a flow 6 of disinfecting liquid is discharged at a predetermined rate. In use, an aqueous sodium chloride solution is fed to the anode chamber at a flow rate 16 to 20% of the product flow rate 6, and water or aqueous sodium chloride is fed through the cathode chamber. Cooling water passed through the inside of the cathode is then fed through inlet 31 to the mixing channel to bring the product solution to the required flow rate and pH level. Hydrogen is channelled to an outlet 36 from within the cathode chamber.
Description
I
Method and Electrolyser for Disinfectant Production The invention belongs to the field of chemical engineering and relates to a method and apparatus for electrolysis of aqueous solution of electrolytes of various concentrations, which can be applied to produce disinfectants, used in the field of health care, biology and ecology. More specifically, the invention deals with electro-chemical technology for producing disinfecting substances by using d iaph rag m-electrolysers.
A number of methods for producing disinfecting substances from anodic electrolysis of aqueous solution of sodium chloride (NaCI), combined with or without cathodic electrolysis for increasing the pH of the disinfecting solution.
Patents RU2079575 [1], RU2297980 [2], W02004/031077 [3] and US2004/0060815 [4] describe methods wherein an electrolyte with equivalent concentration -approximately 10 gIl -is simultaneously channelled into anode and cathode chambers. The anolyte, obtained as electrolyser's output, is a ready to use disinfecting solution, whereas the pH of anolyte can be adjusted to a certain extent by changing the ratio of anolyte and catholyte quantities.
These methods encounter problems as a consequence of the low efficiency of salt for obtaining disinfectant, and as in the case of a number of technologies, high mineralisation of disinfectant will be accompanied by critical accumulation of chlorides in agricultural soil, water circulation pipes of cooling systems, etc. In the case of some other technologies, where large quantities of disinfecting solutions are used (200 cubic metres, on average), for example, municipal water and waste water treatment facilities, high demand for sodium chloride (more than 2 tonnes per day) will decrease the interest in implementing these methods. Decreasing the mineralization of disinfecting substances by increasing the number of electrolysers proportionally will increase the cost of the method and complicate the exploitation of equipment. Total consumption of sodium chloride per 1 gram of active chlorine will be above 12 grams in these methods.
Another material disadvantage is the need for rational use of catolyte, requiring 5-50% water and salt, and which is often discharged -without any effect -into a waste water disposal system.
A method, described in patents RU2088539 [5] and RU2208589 [6] is also known, involving discharging electrolyte with sodium chloride concentration of approximately 10 gIl, in succession, first into cathode chamber and then from cathode chamber to the anode chamber. In the electrolyser's output the anolyte will be a ready-made disinfectant with the approximate pH level of 9.0. The pH level of anolyte can be diminished, if applicable, by discharging some of the catholyte for utilisation before being channelled to anode chamber. The disadvantage of the method described is low efficiency of using sodium chloride -more than 8 grams per 1 gram of active chlorine.
Another method is described in patents RU2148027 [7] and W002/085795 [8], involving channelling electrolyte with the approximate concentration of 2.5 gIl into anode chamber, while concentrated electrolyte with the concentration of 100-300 gIl will enter the cathode chamber from a circulation circuit. The anolyte in the electrolyser's output is a ready-made disinfectant. Approximately 7 grams of sodium chloride will be used per 1 gram of active chlorine. A disadvantage of this method is the use of circulation or the cathode side for cooling and transfer of electrolyte, which further increases the number of narrow passages, which will be covered by cathode sediments.
Methods for acquiring disinfecting solution, described in patent W02006/098660 [9] are known, involving channelling electrolyte at a concentration of up to 2 gIl and 1 gIl, respectively, for single and multiple flow, into an anode chamber, in quantities equal to the disinfectant obtained, not considering the amount of catholyte required to adjust the pH level. Circulating electrolyte from a circuit, which will be mostly filled from electrolyte, out-flowing from the anode chamber, will be discharged into the cathode chamber; the electrolyte will be infiltrated into the circulation circuit through the diaphragm, as the result of a difference in pressure, generated in the anode and cathode chambers. Anolyte, obtained from the output of the electrolyser of the latter, is a product, ready for use. The efficiency of the method is approximately 5.0 grams of sodium chloride per 1 gram of active chlorine, but the implementation of the method is hampered by the need to employ a pressure regulation device and circulation circuit in the anode channel.
A method for obtaining aqueous solutions by anode oxidation of chloride solutions is described in patent RU2088693 [10]; the method is used for water cleaning and disinfecting processes, involving channelling electrolyte -concentrated (up to 300 gIl) sodium chloride solution -into the anode chamber from a circuit, and fresh water based electrolyte into the cathode chamber from the circuit on the cathode side. Gaseous anode product, mostly consisting of chlorine, is discharged from the electrolyser, where it can be mixed with a part of the catholyte and dissolved to the required concentration in fresh water. The method is characterised by high efficiency (salt requirement approximately 3 g per gram), but the disadvantages should be also pointed out -complicated circuits and pressure regulating devices, but also enhanced requirements for sealing of joints and chemical resistance of materials, being in contact with gaseous chlorine.
Patent RU2322397 [11] describes a method for acquiring aqueous solutions of oxidants, where, as it was the case of the method described earlier, concentrated electrolyte is processed in an anode chamber. Mostly gaseous chlorine is produced, as a consequence, and fresh water is charged into cathode chamber, which will be discharged, once treated in cathode chamber, from the electrolyser to be mixed with gaseous chlorine. The presence of highly concentrated gaseous chlorine will restrict the number of possible areas for safe use of the equipment.
As this invention expects the widest implementation of disinfectants developed to take place at the sites where the disinfectants are used most widely (institutions of treatment and preventive care, establishments producing meat, milk, feedingstuffs and other products, farms, swimming pools, water treatment facilities etc.), the method published in patent W02006/098660 (example 2, fig 2), has been chosen for obtaining disinfectants.
In this method, described in the prototype, an aqueous solution of sodium chloride with a concentration of 0.2-2.0 gIl flows through the anode chamber, having the active chlorine concentration of a working solution in the anode chamber and electrolyser output. Electrolyte, infiltrated into the cathode chamber from the anode chamber through a diaphragm, flows through the cathode chamber. Important common characteristics of the prototype and the method, given in the patent application, is slow renewal of electrolyte in the cathode chamber and using fresh water as the starting electrolyte in cathode chamber.
The main disadvantage of the prototype method is the need to maintain a pressure high enough in the anode chamber to ensure a sufficient flow of electrolytes into the cathode chamber, above all, considering the fact that cathode sediments are created on the anode side of the diaphragm. Another disadvantage of the method is the need to increase the pH of acid solution, discharged from anode chamber, to a neutral value of 5.5-7.5, because of high anolyte pressure, using catolyte to meet this objective. Catolyte is dispensed, using the separator type auxiliary equipment.
Technical restrictions on the construction of electrolysers used and low productivity can be highlighted as the main disadvantage of the methods described; this requires the use of auxiliary equipment for increasing efficiency and ensuring the circulation of concentrated electrolyte, for cooling electrolyte and bringing the pH value of used disinfectants to the required neutral value of 5.5-7.5.
The patent RU2350692 [12] provides a detailed description of diaphragm electrolysers with cylindrical flow; this type is used for the implementation of the majority of the methods described above. The largest is capable of producing 25 grams of active chlorine per hour, and therefore the use of the aforementioned electrolysers for mass production purposes is complicated, as more than 150 grams of active chlorine per hour is required there.
A two-chamber coaxial electrolyser with the productivity of up to 150 grams of active chlorine is known from the patent application EE200700021 [13], the main elements of the device being a tubular cathode, diaphragm and anode. The cathode is in an internal position, with the diaphragm between cathode and anode, while the external electrode is an anode, which is coated from the outside with hydro and electrical insulation of red colour. Anode, cathode and diaphragm are fitted, coaxially, with the upper and lower covers, which gives the flow of electrolyte a spiral path; branches of the anode chamber are made into the covers, having the dimensions, which will prevent the anode from being in an area, characterised by enhanced corroding properties, on the boundary of liquid and gaseous stage. The disadvantage of this electrolyser is insufficient productivity -up to 150 grams of active chlorine per hour and the need to use external circulation, cooling and mixing equipment in efficient processes.
A cylindrical diaphragm electrolyser (pending patent application US2009266709 [14]) with assembled anode and assembled diaphragm is chosen as the prototype, having the following main elements: a tubular cathode (internal electrode), diaphragm, anode (external electrode), coated from outside with hydro and electrical insulation of red colour, whereas both the diaphragm and anode are assembled coaxially towards the longitudinal axis, using sleeves with channels for the movement of electrolyte from one end of the anode to the other.
Coaxial construction of electrodes and diaphragm is ensured with lower and upper cover, characterised by the direction of input and output channels, which give the movement of electrolytes along the electrodes a spiral nature. The upper cover has an additional opening for exhausting cathode gases. The electrolyser is capable of producing up to 600 grams of active chlorine per hour under long-term operation. The need to employ external circulation, cooling and mixing devices in efficient processes can be described as the main disadvantage of this electrolyser.
The present invention provides a method and apparatus that can be used to produce disinfectants using an electrolyser and diaphragm to electrolyse anodising products of sodium chloride solution using 3-7 grams of salt per I gram of active chlorine, electrolysers with the productivity of up to 600 grams of active chlorine per device, a simplified hydraulic scheme -compared to processes of comparable efficiency and involving the use of salt -and enhancing the reliability and safety of the equipment.
The invention employs a method for obtaining disinfectants, matching the patent application, involving the electrolysis of sodium chloride solution into anode chamber of electrolyser, whereby the following characteristic parameters must be ensured: fresh water based electrolyte is channelled into the cathode chamber, the quantity being equal to 0.4-0.8% of the quantity of disinfectant obtained, thus providing for high conductivity of the cathode chamber without extra sodium chloride requirement. The catholyte is eliminated from circulation immediately after being discharged from the electrolyser. Intensive conversion of sodium chloride into active chlorine is achieved not by creating high pressure in the anode chamber, but by increasing the hold-up time of electrolyte in anode chamber by cutting the flow through the chamber to 16-20% of the quantity of disinfectant acquired. In this case, the amount of disinfectant shall mean the amount of disinfectant containing 500 mg of active chlorine per liter, i.e., if 720 g of active chlorine compounds is produced per hour in the form of 600 I/h of disinfectant with an active chlorine concentration of 1,200 mg per 1 liter, then the disinfectant amount used for the purposes of calculating the flows through the anode and cathode chamber is not 600 I/hour, but 600x1,2001,440 I/hour.
When these very 720 g per hour are produced, but in the form of 800 I/hour with a concentration of 900 mg per B I liter, the basis for calculation is the same 800x900=1,440 I/hour.
In both cases the flow through the cathode chamber is determined at the rate of 0.4% to 0.8% of 1,440 I/hour, or 4.5 I/hour -9.0 I/hour and the flow through the anode chamber is determined at the rate of 16% to 20% of 1,440 I/hour, or 230 I/hour -288 I/hour.
The anolyte will acquire the concentration of active chlorine in the anode chamber, which is safe for the materials used, and before being discharged from electrolyser, the concentration is taken to a limit, which is recommended for safe use of the disinfectant by the maintenance staff. High-productivity electrolyser is used, ensuring the cooling of small quantities of electrolyte, and bringing the concentration of anolyte to the level required of disinfectants.
The description of the suggested method is the following: disinfectant is obtained from a sodium chloride solution which flows through the anode chamber at the rate of 16-20% of the disinfectant obtained calculated as active chlorine compound concentration of 500mg/I; at the same time electrolyte at a rate of 0.4- 0.8% of the quantity of disinfectant calculated as active chlorine compound concentration of 500 mg/I, flows through the cathode chamber. The remaining fresh water flows through internal space of the internal cathode cooling the electrolyte in the cathode chamber through the cylindrical surface of the cathode and then flows to the electrolyser's cover-mixer input of the through the fresh water output of the cathode. Anolyte, produced in the anode chamber, will be raised to the branch in the anode chamber in the cover-mixer of electrolyser from the space adjacent to the anode, where it is mixed with inflowing water and leaves the electrolyser as a ready-to-use disinfectant. Catholyte is discharged into a utilisation device while hydrogen is discharged into exhaust channels.
The diaphragm electrolyser has the following parts: anode with coaxial location, diaphragm and cathode (anode -external electrode; tubular cathode -internal electrode), monolith covers with inputs for electrolyte and outputs for electrolytic products. The upper cover has two outputs from the cathode chamber -one for catholyte and the other, higher up, for cathode gases. The electrolyser used is characterized by the fact that the tubular cathode has hermetic caps at both ends.
The bottom cover of cathode has a fresh water intake opening, while the upper cover has an output opening. Electrical terminals of the cathode are welded to it, while the upper cover of the electrolyser has an opening for entrance to the branch of the anode chamber or the same side as the disinfectant output opening.
The characterizing parameters of the proposed electrolyser are the following: internal tubular cooling cathode with covers and opening for the inlet and outlet of fresh water, upper cover-mixer with opening to let fresh water into the branch of the anode chamber.
As the consequence of joint implementation of the proposed method and characteristic features of the electrolyser the disinfectant is obtained, under the method set out in claims, by effective use of salt -3.0-7.0 grams of sodium chloride to produce I gram of active chlorine -as the same quantity of sodium chloride in electrolyte will require 5-6 times as much time to pass through the same anode chamber, being conserved as active chlorine more fully. The process is completely safe for both the staff and environment, as the electrolyser is not operating under pressure, while the product of electrolysis is an anolyte, which is obtained as the result of electro-chemical reactions, described with well-known formulas (Elektrochemische Kinetik, Dr Klaus J. Vetter, Springer-Verlag, 1961, §7), and the fluid has active chlorine content up to 3.0 gIl, which is safe for seals, materials and the electrolysers as whole, and involves active chlorine compounds, the main component being hypochlorous acid (HCtO). Before leaving the electrolyser, the concentration of anolyte will be brought to the level characteristic of the concentration of disinfectant, which will be safe for the handling staff. Cathode chamber electrolyte cooling allows a reduction in its amount to the point of acquiring high electric conductivity due to sodium ion migration through the diaphragm and to exclude catholyte circulation in the cooling circuits. Exclusion of a circuit enhances the reliability of the hydraulic scheme and allows the omission of equipment used to create overpressure in the anode channel. Equal pressure in the electrode chambers will facilitate the emergence of a neutral pH level of anolyte and allows the exclusion of a mixing place for anolyte and catholyte from the process. The electrolyser of the invention can be used for the proposed method for achieving high productivity and cutting down maintenance costs, as the use of salt becomes more efficient and the construction of the system is simplified, while the reliability of the system is enhanced and the number of electrolysers, operating simultaneously at the consumer, will be relatively smaller. Decreased mineralization of disinfectant will expand the application of the agent.
The invention will contribute to considerable simplification of the process for obtaining disinfectants and cutting down the related costs, expanding the production range while simplifying the maintenance of production systems and expanding the possible areas of application of the ecological disinfectant thus obtained.
Preferred embodiments of the invention will now be detailed with reference to the accompanying drawings wherein: Figure 1 depicts the hydraulic scheme for a method in accordance with the invention and an electrolyser for implementing the method; Figure 2 depicts the cooling cathode; and Figure 3 shows the cover-mixer.
Figure 1 shows that the hydraulic scheme of the method involves a number of flows: fresh water flow 1 enters an inlet 21 to the cell at a bottom cover 22 of a cylindrical inner cathode 20 and is then transferred though the internal space of cathode 20, up to an upper cover 23 of the cathode 20, and through outlet 24 as flow 2, to an inlet 31 of a cover-mixer 30. Flow 3 will be separated from flow 1 (or flow 2 -not shown here), and enters a sodium chloride mixer 38, where flow 4 is channelled as sodium chloride concentrate, which is then mixed and transferred, as a flow of anode chamber electrolytes 5, into an inlet 41 to a bottom cover of electrolyser 40; the electrolyte will flow along the surface of an outer cylindrical anode 50, through channels 61 in the body of a coupling sleeve 60, axially connecting two anode sections, flowing as anolyte into the branch of anode chamber 32 in the electrolyser's cover-mixer 30, mixing with flow 2, which is flowing towards the channel 33 along the branch's perimeter, and exiting as flow 6 from outlet 34 as a disinfectant for delivery to the consumer. Options are available for filling the cathode chamber through inlet 42 at the bottom cover 40 of the electrolyser. The suitable alternative is chosen, depending on technical feasibility, when choosing the electrolyte for the cathode chamber: if fresh water is used as electrolyte, then the branching should take place at 71 from flow 1 (or flow 2 -not shown here); if the anode chamber electrolyte is also used as the cathode chamber electrolyte, the branching should take place at 72 from flow 5.
Electrolytes with special composition and purpose are transferred as an independent flow 73; the flow of catholyte 8 will be discharged for utilisation or disposal from outlet 35 of the mixer-cover 30; hydrogen will be emitted from outlet 36 into an exhaust system.
Figure 2 depicts a cathode 20, distinguished by being made as an open tube 25, fitted with hermetically sealed covers 22 and 23 with openings 21 and 24, serving as water inlets and outlets, and fitted with electrical terminals 26.
Figure 3 depicts the cover-mixer 30, which has been shown, for the demonstration purposes, assembled in part, with anode 50 and diaphragm 80.
The cover-mixer 30 is fitted with a fresh water inlet 31, which is fitted with outlet 34 at one facet of cover 38; the direction of the channel 37 of inlet 31 matches the spiral movement direction of electrolyte inside the anode chamber; a guiding groove 33 is devised to run along the full perimeter of the cylindrical branch of the anode chamber to facilitate mixing of water and anolyte. The longitudinal axis of groove 33 and centres of openings 31 and 34 are at the same height.
The following examples are being used to substantiate the alternatives for implementing the method of the invention.
Example 1
Example 1 gives the results of method [2], which have been achieved with electrolyser [14], having the geometrical parameters of electrode chambers and the diaphragm, anode, cathode and anode covering materials, which are identical to the electrolyser, developed within the framework of this invention, used in examples 2, 3, 4 and 5. The results of example 1, obtained with the method [2], are used to compare the results of other examples, as the method [2] is widely used, safe, reproducible and similar, outwardly, to the proposed method, as ready to use disinfectant and the catholyte are flowing out from the electrolyser; electrodes are inserted into anode and cathode chamber without any prior electro-chemical treatment and the method is operable without any assistance from auxiliary equipment such as circulation circuits, additional electrolysers and pressure regulating devices in electrode chambers. The results of all the examples are summarised in Table 1.
In example 1, used as comparison, the total flow of water used is mixed with sodium chloride to achieve a concentration of 12 gIl and then separated into two flows: one flow (520 litres per hour) enters the cathode chamber while the other flow (620 litres per hour) enters the anode chamber; the ratio of catholyte and anolyte quantities will meet the interval, given by method [2] -76.5%. Disinfectant is being produced, 680 litres per hour (active chlorine content 850 mg/I, pH 2,4, reduction potential (ORP) 1180 my), using 24.8 g of sodium chloride per I g of active chlorine, the temperature of output solutions will exceed the temperature of water originally used by 26 °C to 30 00.
Example 2
Example 2 gives the results for obtaining disinfectant under minimum flow conditions through the cathode and anode chamber, using the flow rate intervals, specified by this invention. Fresh water is channelled from external source through channel I (the quantity being 1,204 litres per hour (100%)) through the inlet 21 in the cover 22 of cathode 20 to internal space in the cathode, cooling the cathode and also the electrolyte in cathode chamber; after cooling the cathode the fresh water will flow through channel 2, outlet 24 in he cover of 23 to the inlet 31 of cover-mixer 30 in the branch of the anode chamber 32. In the area of channel I or 2 (not really relevant, depending on the construction of the device), before inlet 31, two flows are separated from the fresh water flow: along channel 71 (channels 72 and 73 are missing in this alternative) 4.8 litres of fresh water per hour (0,4%) to the inlet of the cathode chamber; along channel 3 fresh water will be flowing at the rate of 200 litres per hour (16.6%) to the mixer of sodium chloride 38 (the mixer shall be operating, using any recognised method); the liquid then flows, as an electrolyte, with the concentration of 10 g of sodium chlorite per I litre, along channel 5 to the inlet 41 of bottom cover 40 of the electrolyser 10; it flows along anode 50, flowing as anolyte along the channels 61 in the body the coupling sleeve 60 from one consecutive anode chamber to another and will then be directed, as anolyte, having active chlorine concentration of 3 gIl, to the cover-mixer 30 of the branch of anode chamber 32. Anolyte will acquire required concentration on the cover-mixer 30 and will be then transferred as disinfectant to consumers. The catholyte will then flow through channel 8 of outlet 35 to utilisation facility. Hydrogen will be channelled to exhaust through outlet 36. Disinfectant is produced at the rate of 1,200 litres per hour (active chlorine content 510 mg/I, pH 7.25, reduction potential (ORP) 890 my), using 3.33 g of sodium chloride per 1 g of active chlorine, the temperature of output solutions will exceed the temperature of water originally used by 6 00 to 17 00.
Example 3
In example 3 the disinfectant is obtained by allowing the fluids to flow along the same route, which was specified in example 2, but at the maximum flow rates, set out in this invention, through the cathode and anode chambers, respectively, at 0.8% (that is, 10 litres per hour) through he cathode chamber and at 20.6% (that is, 280 litres per hour) through the anode chamber. Disinfectant is produced at the rate of 1,360 litres per hour (active chlorine content 505 mg/I, pH 7,27, reduction potential (ORP) 860 my), using 6.9 g of sodium chloride per I g of active chlorine; the temperature of output solutions will exceed the temperature of water originally used by 5 00 to 15 °C.
Example 4
Example 4 sets out the results for an alternative, where electrolyte arrives along channel 72 to inlet 42; the channel branches off from channel 5 (channels 71 and 73 are missing in this alternative), the quantity being 12 litres per hour (1%), the remaining fluids are flowing along the routes shown in Example 2. For anode treatment, the quantity of arriving fluid is 240 litres per hour (20%), the concentration of both anode and cathode electrolyte being 11.7 g of sodium chloride per I litre. Disinfectant is produced at the rate of 1,200 litres per hour (active chlorine content 500 mg/I, pH 6,2, reduction potential (ORP) 920 my) by using 4.9 g of sodium chloride per 1 g of active chlorine; the temperature of output solutions will exceed the temperature of water originally used by 7 00 to 18 00.
The working name of the disinfectant, produced under the method, involving the use of fresh water, as cathode chamber electrolyte, as described in this invention, is, at the proposal of the authors, ANW -anolyte-neutral-water based; and when using the same solution as the electrolyte of both anode and cathode chamber, ANS -anolyte-neutral-salt based.
Example 5
Example 5 is given for further justification of the concentration range of cathode chamber electrolyte, developed for the purposes of this invention. In Example 5, electrolyte at the concentration of 300 g of sodium chloride per I litre will be flowing along channel 73 (channels 71 and 72 are missing in this alternative) to the cathode chamber; the remaining fluids are flowing along the routes shown in example 2. Disinfectant is produced at the rate of 1,228 litres per hour at the flow rate of 200 litres per hour through the anode chamber and 10.0 litres per hour through the cathode chamber (active chlorine content 545 mg/I, pH 3,4, reduction potential (ORP) 1160 my), using 22.4 g of sodium chloride per 1 g of active chlorine, the temperature of output solutions will exceed the temperature of water originally used by 4 00 to 15 00.
The analysis of implementation results of the methods tells us that increasing the flow rate through the cathode and anode chamber of the same electrolyser, also increasing the sodium chloride concentration in electrolyte in cathode chamber will not impose any restrictions to implementation the method; the analyses shows that optimum results -for the purposes of effectiveness and availability -will be achieved under the flow rates through the cathode and anode chamber, accordingly to the invention, and electrolyte concentration rates, which are entered into cathode and anode chamber.
A useful side effect of the method is the decrease in power consumption for producing I g of active chlorine in all the examples, compared to method [2], assuming the loss through transformers and rectifiers to be approximately 2.1-2.4-fold.
Table I
No Parameter Unit Examples 1 2 3 4 5 1 Quantity of I/hour 680 1200 1357 1200 1228 disinfectant 2 Quantity of catholyte I/hour 520 4.8 10 12 10 3 Waterconsumption I/hour 1200 1205 1367 1212 1228 4 Flow through anode I/hour 680 200 280 240 200 chamber NaCI in catholyte gIl 12.0 --11.7 300 6 NaCI in anode gIl 12.0 10 16.9 11.7 61.0 chamber 7 pH of the unit 2.4 7.25 7.27 6.2 3.4 disinfectant Reduction potential mV 1180 890 860 920 1,160 (ORP) Active chlorine mg/I 850 510 505 500 545 content 8 Total NaCI g/hour 14400 2000 4720 2952 15000 consumption 9 Productivity by g/hour 580 612 684 600 668 active chlorine NaCI consumption g/g 24.8 3.33 6.9 4.92 22.4 for active chlorine 11 Voltage in V 20.9 1OA 11.8 1OA 10.6 electrolyser 12 Current A 600 640 640 600 600 13 Temperature of: Original water °C 22.4 21.5 23.6 21.2 25.0 Catholyte °C 52.0 27.0 29.2 28.0 29.2 Disinfectant °C 48.0 38.0 39.2 39.0 38.6
Claims (7)
- Claims 1. Method for obtaining a disinfectant from aqueous solution of sodium chloride by using diaphragm electrolyser; characterized in that fresh water flow at the rate of 0.4%-0.8% of the obtained disinfectant quantity calculated as active chlorine compound concentration of 500 mg per liter is channelled into the cathode chamber, fresh water flow at the rate of 16%-20% of the obtained disinfectant quantity calculated as active chlorine compound concentration of 500 mg per liter is channelled for mixing with sodium chloride and afterwards the remaning fresh water flow is channelled inside the tubular cathode; fresh water flow is channelled from inside the cathode to the branch of the anode chamber in the cover-mixer of the electrolyse; the flow, originating from the cathode chamber, is discharged for utilisation; the anolyte flow from anode chamber is channelled to the branch of the same anode chamber; the concentration of active chlorine in anolyte is reduced by water supply to the standard level, required of disinfectant, and the disinfectant is discharged from the electrolyser; hydrogen is channelled to the exhaust outlet from the cathode chamber.
- 2. Method according to claim 1, characterized in that the flow entering the cathode chamber is separated from the flow entering the anode chamber only after the sodium chloride mixer.
- 3. Method according to claim 1, characterized in that the flow is channelled into the cathode chamber by means of an independent channel.
- 4. Electrolyser for disinfectant production, which is a cylindrical, flow device of diaphragm type, which comprises following elements: uninterrupted tubular cathode as an internal electrode; anode as an external electrode; diaphragm between the cathode and the anode; monolithic cover-mixer with bottom and upper cover, the covers having a tangentially fitted openings for entering electrolytes and discharging the produce of electrolysis and the upper and bottom cover are fitted with openings for fitting the cathodes, following the direction of axis; the upper cover-mixer includes the branch of the anode chamber and an opening for exhausting hydrogen, which is located higher than the outlet of catolyte; the electrolyser is characterized in that the cathode, having a cover in its bottom part with an inlet for fresh water into the internal space, while the upper cover is fitted with an outlet for discharging fresh water; the upper cover-mixer of the electrolyser has an opening for entering to the branch of the anode chamber, located at the same side with the outlet in the upper cover-mixer of the branch of the anode chamber.
- 5. Electrolyser according to claim 4, characterized in that the anode includes sections, which are connected with each other in succession and along the same axis; the diaphragm includes sections, which are connected with each other in succession and along the same axis; the sections of the anode and diaphragm are connected in succession, along the same axis and with coaxial coupling sleeves, while the bodies of the coupling sleeves are fitted with channels, allowing the electrolyte to flow from one section of the anode to another.
- 6. Electrolyser according to claims 4 and, characterized in that the inlet of the branch of the anode chamber in the upper cover-mixer of the electrolyser is at the same height with the outlet of the upper cover-mixer of the branch of the anode chamber.
- 7. Electrolyser according to claims 4 and 5, characterized in that a groove is made along the perimeter of the cylindrical part of the upper cover-mixer of the branch of the anode chamber, fitted at the same height with the inlets and outlets of the anode chamber.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EEP201000069A EE05607B1 (en) | 2010-09-09 | 2010-09-09 | Method and electrolyte serum for disinfectant |
Publications (2)
Publication Number | Publication Date |
---|---|
GB201115467D0 GB201115467D0 (en) | 2011-10-26 |
GB2483555A true GB2483555A (en) | 2012-03-14 |
Family
ID=44908217
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB1115467.1A Withdrawn GB2483555A (en) | 2010-09-09 | 2011-09-07 | Diaphragm Electrolyser for Disinfectant Production |
Country Status (4)
Country | Link |
---|---|
US (2) | US8568574B2 (en) |
EE (1) | EE05607B1 (en) |
GB (1) | GB2483555A (en) |
RU (1) | RU2566747C2 (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
IT201600127542A1 (en) * | 2016-12-16 | 2018-06-16 | Pica Mario | "ELECTROLYTIC CELL FOR THE PRODUCTION OF DETERGENT OR DISINFECTANT LIQUIDS" |
WO2018109748A1 (en) * | 2016-12-16 | 2018-06-21 | PICA, Mario | Method and electrolytic cell for the production of detergents and disinfectants liquids |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EE05608B1 (en) * | 2010-12-30 | 2012-12-17 | Ilt�enko Valeri | Method and apparatus for obtaining a disinfectant |
RU2503173C1 (en) * | 2012-08-14 | 2014-01-10 | Государственное научное учреждение Всероссийский научно-исследовательский институт мясного скотоводства Российской академии сельскохозяйственных наук | Flow-through electrolytic cell of module type |
EE05823B1 (en) | 2015-02-27 | 2020-07-15 | IltEnko Valeri | Diaphragm-electrolyser |
KR102745204B1 (en) * | 2018-02-09 | 2024-12-23 | 엘지전자 주식회사 | sterilizing water generation apparatus |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5783052A (en) * | 1996-03-11 | 1998-07-21 | Rscecat, Usa, Inc. | Electrochemical cell |
EP1538128A2 (en) * | 2003-12-04 | 2005-06-08 | Aquastel International B.V. | End cap for an electrolytic cell |
GB2468928A (en) * | 2008-04-23 | 2010-09-29 | Valeri Iltsenko | Cylindrical coaxial electrolytic cell with segmented anode and diaphragm |
Family Cites Families (16)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP3327922B2 (en) * | 1991-02-14 | 2002-09-24 | マテリアルズ・リサーチ・ピーティーワイ・リミテッド | Metal recovery equipment |
RU2079575C1 (en) | 1995-05-31 | 1997-05-20 | Витольд Михайлович Бахир | Apparatus for production of washing and disinfection solution |
RU2088539C1 (en) | 1995-05-31 | 1997-08-27 | Витольд Михайлович Бахир | Apparatus for producing detergent and disinfecting solutions |
RU2088693C1 (en) | 1996-02-09 | 1997-08-27 | Витольд Михайлович Бахир | Installation for preparing products of anode oxidation of alkali and alkali-earth metal chloride solution |
RU2148027C1 (en) | 1999-02-01 | 2000-04-27 | Бахир Витольд Михайлович | Method of preparing disinfecting solution in the form of neutral anodic liquor |
DE60036582T2 (en) | 1999-08-06 | 2008-06-26 | Puricore International Ltd. | Electrochemical treatment of an aqueous solution |
RU2241683C2 (en) | 2001-04-24 | 2004-12-10 | Габленко Вячеслав Георгиевич | Method of synthesis of oxidizers from the water solution of sodium chloride and a device for its realization |
RU2208589C2 (en) | 2001-08-03 | 2003-07-20 | Бахир Витольд Михайлович | Method of production of disinfecting solution and device for method embodiment |
GB2393737B (en) | 2002-10-03 | 2005-08-17 | Sterilox Tech Int Ltd | Electronic treatment of an aqueous salt solution |
RU2005107362A (en) | 2005-03-17 | 2006-08-27 | Витольд Михайлович Бахир (RU) | METHOD FOR REDUCING CORROSION ACTIVITY OF AQUEOUS CHLORINE-CONTAINING SOLUTIONS AND A DISINFECTANT |
RU2297980C1 (en) | 2005-11-30 | 2007-04-27 | Государственное учреждение Волгоградский научно-исследовательский технологический институт мясо-молочного скотоводства и переработки продукции животноводства Россельхозакадемии (ГУ ВНИТИ ММС и ППЖ Россельхозакадемии) | Method of the electroactivation of the water solutions |
US7374645B2 (en) * | 2006-05-25 | 2008-05-20 | Clenox, L.L.C. | Electrolysis cell assembly |
RU2322397C1 (en) | 2006-08-25 | 2008-04-20 | Витольд Михайлович Бахир | Device for producing water solution of oxidants |
EE05447B1 (en) | 2007-04-30 | 2011-08-15 | Ilt�enko Valeri | Processor for dual chamber coaxial electrolyzer |
RU2350692C1 (en) | 2007-07-10 | 2009-03-27 | Витольд Михайлович Бахир | Electrochemical modular cell for processing of electrolytes solutions |
EE05494B1 (en) | 2008-04-23 | 2011-12-15 | Valeri Iltshenko | Cylindrical diaphragm electrolyte with anode assembly and diaphragm |
-
2010
- 2010-09-09 EE EEP201000069A patent/EE05607B1/en unknown
-
2011
- 2011-01-18 US US13/008,742 patent/US8568574B2/en active Active
- 2011-08-16 RU RU2011134294/04A patent/RU2566747C2/en active
- 2011-09-07 GB GB1115467.1A patent/GB2483555A/en not_active Withdrawn
-
2013
- 2013-09-25 US US14/036,987 patent/US9340883B2/en active Active
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5783052A (en) * | 1996-03-11 | 1998-07-21 | Rscecat, Usa, Inc. | Electrochemical cell |
EP1538128A2 (en) * | 2003-12-04 | 2005-06-08 | Aquastel International B.V. | End cap for an electrolytic cell |
GB2468928A (en) * | 2008-04-23 | 2010-09-29 | Valeri Iltsenko | Cylindrical coaxial electrolytic cell with segmented anode and diaphragm |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
IT201600127542A1 (en) * | 2016-12-16 | 2018-06-16 | Pica Mario | "ELECTROLYTIC CELL FOR THE PRODUCTION OF DETERGENT OR DISINFECTANT LIQUIDS" |
WO2018109748A1 (en) * | 2016-12-16 | 2018-06-21 | PICA, Mario | Method and electrolytic cell for the production of detergents and disinfectants liquids |
CN110325668A (en) * | 2016-12-16 | 2019-10-11 | 马里奥·皮卡 | Method and electrolyzer for the production of detergent and disinfectant liquids |
US11174562B2 (en) | 2016-12-16 | 2021-11-16 | Igor BUT | Method and electrolytic cell for the production of detergents and disinfectants liquids |
CN110325668B (en) * | 2016-12-16 | 2022-07-29 | 马里奥·皮卡 | Method and electrolytic cell for producing detergent and disinfectant liquids |
Also Published As
Publication number | Publication date |
---|---|
RU2011134294A (en) | 2013-02-27 |
US20120061254A1 (en) | 2012-03-15 |
US20140021061A1 (en) | 2014-01-23 |
EE05607B1 (en) | 2012-12-17 |
GB201115467D0 (en) | 2011-10-26 |
US8568574B2 (en) | 2013-10-29 |
US9340883B2 (en) | 2016-05-17 |
EE201000069A (en) | 2012-04-16 |
RU2566747C2 (en) | 2015-10-27 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US9340883B2 (en) | Method and electrolyser for disinfectant production | |
US11851353B2 (en) | Electrolytic cell and system for treating water | |
CA1197489A (en) | Electrolytic swimming pool chlorination | |
US20100140080A1 (en) | Method and apparatus for making electrolyzed water | |
US20130146473A1 (en) | Dual diaphragm electrolysis cell assembly and method for generating a cleaning solution without any salt residues and simultaneously generating a sanitizing solution having a predetermined level of available free chlorine and pH | |
CN110325668B (en) | Method and electrolytic cell for producing detergent and disinfectant liquids | |
CN102010035A (en) | Immersed electrolysis mixing device | |
US9797050B2 (en) | Energy-efficient diaphragm-electrolyser | |
JP2012067356A (en) | Apparatus and method for producing hypochlorous acid water | |
KR101903387B1 (en) | Electric Device | |
KR102104511B1 (en) | Sterilization device for small scale water supply facility | |
CN202039131U (en) | Immersed electrolyzing mixing device | |
CN101891153A (en) | Chlorine dioxide compound disinfectant generator and using method thereof | |
KR20140034305A (en) | Electrolyzed water production device | |
RU2454489C1 (en) | Electrochemical cell for treatment of electrolyte solutions | |
CN216006029U (en) | Electrolytic tank for manufacturing subacidity hypochlorous acid | |
CN105112933B (en) | A kind of high yield chlorine electrolysis unit | |
CN105274553B (en) | Half diaphragm hypochlorite generator | |
CN111003756B (en) | Efficient composite electrolytic disinfection device for tail end of tap water plant | |
CN203913156U (en) | Agricultural generates machine by ecological property bactericidal liquid | |
RU2729184C1 (en) | Electrochemical reactor and apparatus for electrochemical synthesis of a mixture of oxidants | |
US20230226502A1 (en) | Method and apparatus for producing chlorine gas in an electrolytic cell | |
RU37985U1 (en) | PORTABLE DEVICE FOR ELECTROCHEMICAL LIQUID TREATMENT | |
CN113429040A (en) | Movable environment-friendly multifunctional emergency disinfection device | |
KR20200089325A (en) | Method and apparatus for oxidant concentration control |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
WAP | Application withdrawn, taken to be withdrawn or refused ** after publication under section 16(1) |